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CDD-787

Chemical Structure : CDD-787

CAS No.: 2822750-93-4

CDD-787 (CDD787)

Catalog No.: PC-38775Not For Human Use, Lab Use Only.

CDD-787 is a highly potent, selective BET bromodomain 1 (BET BD1) inhibitor with IC50 of 2.1 and 3.3 nM for BRDT-BD1 and BRD4-BD1, respectively, with high selectivity (>3,000-fold) over BET BD2 proteins.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

CDD-787 is a highly potent, selective BET bromodomain 1 (BET BD1) inhibitor with IC50 of 2.1 and 3.3 nM for BRDT-BD1 and BRD4-BD1, respectively, with high selectivity (>3,000-fold) over BET BD2 proteins.
CDD-787 exhibits picomolar inhibition against BRD2-BDT1 (IC50 260 pM), BRD3-BD1 (IC50 130 pM), BRD4-BD1 (IC50 290 pM), and BRDT-BD1 (IC50 220 pM), respectively, in the bromoKdELECT assays.
CDD-787 inhibited cell viability of MV4;11 and MOLM-13 cells with IC50 of 8.3 nM and 16 nM, respectively.
CDD-787 induced G1 arrest and apoptosis in both MV4;11 and MOLM-13 cells, suppressed MYC expression in both cell lines.

Physicochemical Properties

M.Wt 593.728
Formula C35H39N5O4
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(R)-5-(2,4-dimethylphenyl)-N-(3-(1-(2-(4-methyl-2-oxo-1,2-dihydroquinolin-6-yl)acetyl)piperidin-4-yl)-1-(methylamino)-1-oxopropan-2-yl)picolinamide

References

1. Modukuri RK, et al. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2122506119.

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